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| Product NDC Code | 20276-047 | ||||||||
|---|---|---|---|---|---|---|---|---|---|
| Drug Name | Lucky dry hair |
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| Type | Brand | ||||||||
| Active Ingredients |
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| Route | TOPICAL | ||||||||
| Dosage Form | SHAMPOO | ||||||||
| RxCUI drug identifier | 1052932 | ||||||||
| Application Number | M032 | ||||||||
| Labeler Name | Delta Brands Inc | ||||||||
| Packages |
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| Check if available Online | Get Medication Prices online with Discount |
Active ingredient
A list of the active, medicinal ingredients in the drug product.Active Ingredient Pyrithione zinc 0.3%
Dosage and administration
Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.Directions •wet hair, •squeeze small amount into palm •lather, •rinse well
Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.Inactive Ingredients acrylates copolymer, benzyl alcohol, cocamidopropyl betaine, cocamide DEA, cocamide MEA, coco glucoside, FDC blue no. 1, fragrance, glycol distearate, laureth 10, methylchloroisothiazolinone, methylisothiazolinone,polyquarternium 10, sodium chloride, sodium laureth sulfate, styrene/acrylates copolymer, tetrasodium EDTA, triethanolamine, water, zinc sulfate
Indications and usage
A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.Uses • helps to treat flakes, itch, irritation, oilness or dryness caused by dandruff.
Purpose
Information about the drug product’s indications for use.Purpose Anti-dandruff
Spl product data elements
Usually a list of ingredients in a drug product.Lucky Dry Hair pyrithione zinc BENZYL ALCOHOL COCAMIDOPROPYL BETAINE COCO DIETHANOLAMIDE COCO MONOETHANOLAMIDE COCO GLUCOSIDE FD&C BLUE NO. 1 GLYCOL DISTEARATE LAURETH-10 METHYLCHLOROISOTHIAZOLINONE METHYLISOTHIAZOLINONE POLYQUATERNIUM-10 (400 CPS AT 2%) SODIUM CHLORIDE SODIUM LAURETH SULFATE EDETATE SODIUM TROLAMINE WATER ZINC SULFATE PYRITHIONE ZINC PYRITHIONE ZINC
Package label principal display panel
The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.Package Label Package Label
Keep out of reach of children
Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.Keep out of reach of children Keep this and all drugs out of reach of children If swallowed get medical help or contact a Poison Control Center right away.
Stop use
Information about when use of the drug product should be discontinued immediately and a doctor consulted. Includes information about any signs of toxicity or other reactions that would necessitate immediately discontinuing use of the product.Stop use and ask a doctor if condition does not improve or worsen after regular use of this product as directed
When using
Information about side effects that people may experience, and the substances (e.g. alcohol) or activities (e.g. operating machinery, driving a car) to avoid while using the drug product.When using this product •avoid contact with eyes • if contact occurs, rinse eyes with plenty of water.
Warnings
Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.Warnings For external use only
Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API